@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP63185.RAtBd1ZPGYoWo29vLuVOdqUr2H7bJ8WjOXoQiJFo-v2vE
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP63185.RAtBd1ZPGYoWo29vLuVOdqUr2H7bJ8WjOXoQiJFo-v2vE130_head
{
this:
np:hasAssertion
dgn-np:NP63185.RAtBd1ZPGYoWo29vLuVOdqUr2H7bJ8WjOXoQiJFo-v2vE130_assertion
;
np:hasProvenance
dgn-np:NP63185.RAtBd1ZPGYoWo29vLuVOdqUr2H7bJ8WjOXoQiJFo-v2vE130_provenance
;
np:hasPublicationInfo
dgn-np:NP63185.RAtBd1ZPGYoWo29vLuVOdqUr2H7bJ8WjOXoQiJFo-v2vE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP63185.RAtBd1ZPGYoWo29vLuVOdqUr2H7bJ8WjOXoQiJFo-v2vE130_assertion
a
np:Assertion
.
dgn-np:NP63185.RAtBd1ZPGYoWo29vLuVOdqUr2H7bJ8WjOXoQiJFo-v2vE130_provenance
a
np:Provenance
.
dgn-np:NP63185.RAtBd1ZPGYoWo29vLuVOdqUr2H7bJ8WjOXoQiJFo-v2vE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP63185.RAtBd1ZPGYoWo29vLuVOdqUr2H7bJ8WjOXoQiJFo-v2vE130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0345904
a
ncit:C7057
.
dgn-gda:DGNc690f6687d03af008a26dbcefcbd0288
sio:SIO_000628
miriam-gene:3077
,
lld:C0345904
;
a
sio:SIO_001122
.
}
dgn-np:NP63185.RAtBd1ZPGYoWo29vLuVOdqUr2H7bJ8WjOXoQiJFo-v2vE130_provenance
{
dgn-np:NP63185.RAtBd1ZPGYoWo29vLuVOdqUr2H7bJ8WjOXoQiJFo-v2vE130_assertion
dcterms:description
"[ The mutation of C282Y may be related with susceptibility to HCC after chronic hepatitis B. This outcome suggests that host HFE mutation may be an important factor related to the pathogenesis of HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:16174459
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP63185.RAtBd1ZPGYoWo29vLuVOdqUr2H7bJ8WjOXoQiJFo-v2vE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}